Package 68071-4722-9

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4722-9
Digits Only 6807147229
Product NDC 68071-4722
Product ID 68071-4722_1aba0ea7-cfd7-d3e1-e063-6394a90a08f8
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-4722-9)

Marketing

Marketing Status
Marketed Since 2019-01-22
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Benazepril Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1aba0ea7-cfd7-d3e1-e063-6394a90a08f8", "openfda": {"upc": ["0368071472295"], "unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["800f2a14-98b9-3499-e053-2991aa0a197d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-4722-9)", "package_ndc": "68071-4722-9", "marketing_start_date": "20190122"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-4722_1aba0ea7-cfd7-d3e1-e063-6394a90a08f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-4722", "generic_name": "Benazepril Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}